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Organic Letters|October 22, 2004
Asymmetric catalytic synthesis of enantiopure N-protected 1,2-amino alcoholsGiuseppe Bartoli, Marcella Bosco, Armando Carlone, et al.The Journal of Organic Chemistry|April 13, 2002
Conformational studies by dynamic NMR. 88.(1) stereomutation processes in the diastereoisomers of a representative amino alcohol and related amide precursorsGiuseppe Bartoli, Stefano Grilli, Lodovico Lunazzi, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|April 17, 2010
Controlling stereoselectivity in the aminocatalytic enantioselective Mannich reaction of aldehydes with in situ generated N-carbamoyl iminesPatrizia Galzerano, Dario Agostino, Giorgio Bencivenni, et al.The Journal of Organic Chemistry|February 14, 2004
Investigation into the allylation reactions of aldehydes promoted by the CeCl3.7H2O-NaI system as a Lewis acidGiuseppe Bartoli, Marcella Bosco, Arianna Giuliani, et al.Organic Letters|June 18, 2004
Asymmetric aminolysis of aromatic epoxides: a facile catalytic enantioselective synthesis of anti-beta-amino alcoholsGiuseppe Bartoli, Marcella Bosco, Armando Carlone, et al.Chemical Communications (Cambridge, England)|March 30, 2007
Organocatalytic asymmetric hydrophosphination of nitroalkenesGiuseppe Bartoli, Marcella Bosco, Armando Carlone, et al.The Journal of Organic Chemistry|December 16, 2006
Alcohols and di-tert-butyl dicarbonate: how the nature of the Lewis acid catalyst may address the reaction to the synthesis of tert-butyl ethersGiuseppe Bartoli, Marcella Bosco, Armando Carlone, et al.Organic & Biomolecular Chemistry|June 10, 2010
A convergent approach to (R)-Tiagabine by a regio- and stereocontrolled hydroiodination of alkynesGiuseppe Bartoli, Roberto Cipolletti, Giustino Di Antonio, et al.The Journal of Organic Chemistry|December 7, 2002
Simple and efficient chemoselective mild deprotection of acetals and ketals using cerium(III) triflateRenato Dalpozzo, Antonio De Nino, Loredana Maiuolo, et al.The Journal of Organic Chemistry|February 13, 2008
Efficient transformation of azides to primary amines using the mild and easily accessible CeCl3.7H2O/NaI systemGiuseppe Bartoli, Giustino Di Antonio, Riccardo Giovannini, et al.Pageof 3